Effect of an external electric field on the electron paramagnetic resonance (EPR) spectra of Gd3+ ions and the types of impurity centers in zinc tungstate single crystals

1970 ◽  
Vol 11 (2) ◽  
pp. 247-250 ◽  
Author(s):  
G. B. Bokii ◽  
I. A. Gavrilov ◽  
A. T. Sobolev ◽  
V. B. Kravchenko ◽  
O. F. Dudnik ◽  
...  
Open Physics ◽  
2012 ◽  
Vol 10 (2) ◽  
Author(s):  
Grzegorz Leniec ◽  
Tomasz Skibiński ◽  
Slawomir Kaczmarek ◽  
Przemyslaw Iwanowski ◽  
Marek Berkowski

AbstractGrowth conditions and electron paramagnetic resonance investigations of two well oriented KSm(WO4)2 and KEr(WO4)2 single crystals have been presented and discussed. Hyperfine structure of Sm3+ ion was detected and analyzed for angular and temperature dependences. EPR spectra of KEr(WO4)2 and its angular dependence showed the presence of 5 magnetically nonequivalent Er centers in the crystal. A change in the type of magnetic interactions was analyzed using mixed (Gaussian and Lorentzian) fits of the EPR spectra.


2017 ◽  
Vol 121 (30) ◽  
pp. 16533-16540 ◽  
Author(s):  
Mantas Šimėnas ◽  
Anastasia Kultaeva ◽  
Sergejus Balčiu̅nas ◽  
Monika Trzebiatowska ◽  
Daniel Klose ◽  
...  

1999 ◽  
Vol 54 (8-9) ◽  
pp. 557-558 ◽  
Author(s):  
F. Köksal ◽  
Ş. Bahadir ◽  
E. Başaran ◽  
Y. Yerli

Electron paramagnetic resonance of [(CH3)4N]2MnCl4 and [(CH3)4N]2FeCl4 single crystals was studied between 20 and 400 K. The peak-to-peak derivative linewidths of these crystals seem not to change in this temperature interval and approximately 100 mT for [(CH3)4N]2MnCl4 and ~20 mT for [(CH3)4N]2FeCl4 .The spectra were found to be isotropic, with g = 2.0039 for [(CH3)4N]2MnCl4 and g = 2.0042 for [(CH3)4N]2FeCl4 .This temperature independence is attributed to isotropic strong ex-change interactions of Mn2- and Fe2+ nuclei, and it seems that hindered rotation of the MnCl42- and FeCl42- tetrahedra does not occur in this temperature interval.


1996 ◽  
Vol 51 (4) ◽  
pp. 245-248
Author(s):  
Geetha Jayaram ◽  
V. G. Krishnan

Abstract Electron Paramagnetic Resonance (EPR) studies have been carried out on the vanadyl (VO2) ion doped in single crystals of ZnTiF6 • 6H2O. The spectra indicate the presence of one set of eight lines characteristic of only one occupation site. The V-O bond orientation is along one of the three Zn-H2O bond directions in the trigonally distorted [Zn(H2O)6] octahedra. This behaviour is unlike that reported for vanadyl ion substituting for the M(H2O)6 sites in the Tutton salts, alums and AlCl3 • 6H2O. The Spin-Hamiltonian and bonding parameters for the [VO(H2O)5] complex have been evaluated. The hyperfine linewidths are 0.8 mT at 300 K and 77 K. No proton superhyperfine structure was observed at both these temperatures.


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